HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101421777A>G , CM000671.2:g.101421777A>G | GRCh38 |
NC_000009.11:g.104184059A>G , CM000671.1:g.104184059A>G | GRCh37 |
NC_000009.10:g.103223880A>G | NCBI36 |
NG_012387.1:g.19004T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647789.2:c.*32T>C MANE Select | ENSP00000497767.1:n.*32T>C | |
ENST00000648064.1:c.*32T>C | ENSP00000497990.1:n.*32T>C | |
ENST00000648758.1:c.*32T>C | ENSP00000497731.1:n.*32T>C | |
ENST00000374855.8:c.*32T>C | ENSP00000363988.4:n.*32T>C | |
ENST00000616752.1:c.*139T>C | ENSP00000481363.1:n.*139T>C | |
NM_000035.3:c.*32T>C | NP_000026.2:n.*32T>C | |
NM_000035.4:c.*32T>C MANE Select | NP_000026.2:n.*32T>C |